@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP675560.RA1yPQzNAWXDLk5rty5JprW47Yb93NbLWCHeVBmUNQ4Jg
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP675560.RA1yPQzNAWXDLk5rty5JprW47Yb93NbLWCHeVBmUNQ4Jg130_head
{
this:
np:hasAssertion
dgn-np:NP675560.RA1yPQzNAWXDLk5rty5JprW47Yb93NbLWCHeVBmUNQ4Jg130_assertion
;
np:hasProvenance
dgn-np:NP675560.RA1yPQzNAWXDLk5rty5JprW47Yb93NbLWCHeVBmUNQ4Jg130_provenance
;
np:hasPublicationInfo
dgn-np:NP675560.RA1yPQzNAWXDLk5rty5JprW47Yb93NbLWCHeVBmUNQ4Jg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP675560.RA1yPQzNAWXDLk5rty5JprW47Yb93NbLWCHeVBmUNQ4Jg130_assertion
a
np:Assertion
.
dgn-np:NP675560.RA1yPQzNAWXDLk5rty5JprW47Yb93NbLWCHeVBmUNQ4Jg130_provenance
a
np:Provenance
.
dgn-np:NP675560.RA1yPQzNAWXDLk5rty5JprW47Yb93NbLWCHeVBmUNQ4Jg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP675560.RA1yPQzNAWXDLk5rty5JprW47Yb93NbLWCHeVBmUNQ4Jg130_assertion
{
miriam-gene:3815
a
ncit:C16612
.
lld:C0024299
a
ncit:C7057
.
dgn-gda:DGN08c56b0cb8edd04c93ac30790e5690ac
sio:SIO_000628
miriam-gene:3815
,
lld:C0024299
;
a
sio:SIO_001121
.
}
dgn-np:NP675560.RA1yPQzNAWXDLk5rty5JprW47Yb93NbLWCHeVBmUNQ4Jg130_provenance
{
dgn-np:NP675560.RA1yPQzNAWXDLk5rty5JprW47Yb93NbLWCHeVBmUNQ4Jg130_assertion
dcterms:description
"[Mutations causing constitutive activation of KIT have been shown to be causative in some forms of mastocytosis, and several types of mutations have been associated with myeloproliferative disorders (MPDs), acute myelogenous leukemia (AML), sinonasal lymphomas, and gastrointestinal stromal tumors (GIST).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:11377682
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP675560.RA1yPQzNAWXDLk5rty5JprW47Yb93NbLWCHeVBmUNQ4Jg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:47+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}